IP Library Granted Patent US 8,475,792
Granted Patent B2
US 8,475,792 · App. 13/659,144 · Granted Jul 2, 2013

Molecules with extended half-lives, compositions and uses thereof

Inventors: William Dall'Acqua (Gaithersburg, MD); Leslie S. Johnson (Darnestown, MD); Elizabeth Sally Ward Ober (Dallas, TX)
Assignees: MedImmune, LLC; Board of Regents, The Texas University System
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,475,792
App. No.
13/659,144
Granted
Jul 2, 2013
Kind
B2
Abstract

The present invention provides molecules, including IgGs, non-IgG immunoglobulins, proteins and non-protein agents, that have increased in vivo half-lives due to the presence of an IgG constant domain, or a portion thereof that binds the FcRn, having one or more amino acid modifications that increase the affinity of the constant domain or fragment for FcRn. Such proteins and molecules with increased half-lives have the advantage that smaller amounts and or less frequent dosing is required in the therapeutic, prophylactic or diagnostic use of such molecules.

Claims (32)

1. A fusion protein comprising a non-IgG polypeptide covalently linked to a modified human IgG constant domain, or a fragment thereof that binds to FeRn, said modified human IgG constant domain or fragment comprising one or more amino acid modifications relative to a wild-type human IgG constant domain, wherein the one or more modifications are at one or more of positions 251-256, 285-290, 308-314, 385-389, and 428-436, numbered according to the EU numbering index of Kabat, and wherein at least one of the one or more modifications is an insertion, deletion or substitution, and wherein said fusion protein has a longer half life than the non-IgG polypeptide alone.

2. The fusion protein according to claim 1 , wherein at least one of the one or more amino acid modifications is a substitution with tyrosine, tryptophan, threonine, serine or phenylalanine at position 252, substitution with threonine at position 254, substitution with glutamine, arginine, serine, aspartic acid or glutamic acid at position 256, substitution with proline at position 309, substitution with serine at position 311, substitution with arginine, aspartic acid, threonine, histidine, lysine, alanine, glycine, or serine at position 385, substitution with threonine, aspartic acid, serine, lysine, arginine, isoleucine, methionine or proline at position 386, substitution with arginine, histidine, serine, threonine, alanine or proline at position 387, substitution with proline, asparagine or serine at position 389, substitution with threonine, leucine, phenylalanine or serine at position 428, substitution with histidine, tyrosine or phenylalanine at position 434, substitution with arginine, isoleucine, proline, glutamine or serine at position 433, or substitution with histidine, arginine, asparagine, lysine, methionine or threonine at position 436.

3. A molecule comprising a non-protein agent conjugated to a modified human IgG constant domain, or a fragment thereof that binds to FcRn, said modified human IgG constant domain or fragment comprising one or more amino acid modifications relative to a wild-type human IgG constant domain, wherein the one or more modifications are at one or more of positions 251-256, 285-290, 308-314, 385-389, and 428-436, numbered according to the EU numbering index of Kabat, and wherein at least one of the one or more modifications is an insertion, deletion or substitution, and wherein said molecule has a longer half life than the non-protein agent alone.

4. A pharmaceutical composition comprising the fusion protein according to claim 1 and a pharmaceutically acceptable carrier.

5. A pharmaceutical composition comprising the molecule according to claim 3 and a pharmaceutically acceptable carrier.

6. The fusion protein according to claim 1 , wherein the one or more amino acid modifications are substitutions at positions 252, 254, and 256.

7. The fusion protein according to claim 6 , wherein the substitution at position 252 is a substitution with a tyrosine, the substitution at position 254 is a substitution with a threonine, and the substitution at position 256 is a substitution with a glutamic acid.

8. The fusion protein according to claim 1 , wherein the one or more amino acid modifications is a substitution at position 428.

9. The fusion protein according to claim 8 , wherein the substitution at position 428 is a substitution with threonine, leucine, phenylalanine or serine.

10. The fusion protein according to claim 1 , wherein the one or more amino acid modifications are one or more substitutions at positions 252, 254, or 256 and wherein the one or more substitutions is:

a tyrosine, a phenylalanine, serine, tryptophan or threonine amino acid substitution at position 252;

a threonine amino acid substitution at position 254: or

a serine, arginine, glutamine, glutamic acid or aspartic acid amino acid substitution at position 256.

11. The fusion protein according to claim 1 , wherein the one or more amino acid modifications are one or more substitutions at positions 433, 434 or 436 and wherein the one or more substitutions is:

an arginine, serine, isoleucine, proline, or glutamine amino acid substitution at amino acid residue 433;

a histidine, phenylalanine or tyrosine amino acid substitution at amino acid residue 434: or

a histidine, asparagine, arginine, threonine, lysine or methionine amino acid residue 436.

12. The fusion protein according to claim 1 , wherein the one or more amino acid modifications are substitutions at positions 433, 434 and 436, and wherein the substitution at position 433 is a substitution with a lysine, the substitution at position 434 is substitution with a phenylalanine, and the substitution at position 436 is a substitution with a histidine.

13. The molecule according to claim 3 , wherein at least one of the one or more amino acid modifications is a substitution with tyrosine, tryptophan, threonine, serine or phenylalanine at position 252, substitution with threonine at position 254, substitution with glutamine, arginine, serine, aspartic acid or glutamic acid at position 256, substitution with proline at position 309, substitution with serine at position 311, substitution with arginine, aspartic acid, threonine, histidine, lysine, alanine, glycine, or serine at position 385, substitution with threonine, aspartic acid, serine, lysine, arginine, isoleucine, methionine or proline at position 386, substitution with arginine, histidine, serine, threonine, alanine or proline at position 387, substitution with proline, asparagine or serine at position 389, substitution with threonine, leucine, phenylalanine or serine at position 428, substitution with histidine, tyrosine or phenylalanine at position 434, substitution with arginine, isoleucine, proline, glutamine or serine at position 433, or substitution with histidine, arginine, asparagine, lysine, methionine or threonine at position 436.

14. The molecule according to claim 3 , wherein the one or more amino acid modifications are substitutions at positions 252, 254, and 256.

15. The molecule according to claim 14 , wherein the substitution at position 252 is a substitution with a tyrosine, the substitution at position 254 is a substitution with a threonine, and the substitution at position 256 is a substitution with a glutamic acid.

16. The molecule according to claim 3 , wherein the one or more amino acid modifications is a substitution at position 428.

17. The fusion protein according to claim 16 , wherein the substitution at position 428 is a substitution with threonine, leucine, phenylalanine or serine.

18. The fusion protein according to claim 3 , wherein the one or more amino acid modifications are one or more substitutions at positions 252, 254, or 256 and wherein the one or more substitutions is:

a tyrosine, a phenylalanine, serine, tryptophan or threonine amino acid substitution at position 252;

a threonine amino acid substitution at position 254; or

a serine arginine, glutamine, glutamic acid or aspartic acid amino acid substitution at position 256.

19. The fusion protein according to claim 3 , wherein the one or more amino acid modifications are one or more substitutions at positions 433, 434 or 436 and wherein the one or more substitutions is:

an arginine, serine, isoleucine, proline, or dutamine amino acid substitution at amino acid residue 433;

a histidine, phenylalanine or tyrosine amino acid substitution at amino acid residue 434; or

a histidine, asparagine, arginine, threonine, lysine or methionine amino acid residue 436.

20. The fusion protein according to claim 3 , wherein the one or more amino acid modifications are substitutions at positions 433, 434 and 436, and wherein the substitution at position 433 is a substitution with a lysine, the substitution at position 434 is substitution with a phenylalanine, and the substitution at position 436 is a substitution with a histidine.

Assignments (5)
CONFIRMATORY LICENSE Recorded Feb 4, 2021
From: UT SOUTHWESTERN MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 055221/0714 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNEE ON THE COVER SHEET, MISTAKENLY REPRESENTED AS "BOARD AND REGENTS, THE UNIVERSITY OF TEXAS SYSTEM" PREVIOUSLY RECORDED ON REEL 030308 FRAME 0316. ASSIGNOR(S) HEREBY CONFIRMS THE CORRECT NAME OF THE ASSIGNEE IS "BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM.". Recorded May 17, 2013
From: WARD OBER, ELIZABETH SALLY
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 030440/0782 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2013
From: WARD OBER, ELIZABETH SALLY
To: BOARD AND REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 030308/0316 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2013
From: DALL'ACQUA, WILLIAM; JOHNSON, LESLIE S.
To: MEDIMMUNE, INC.
Reel/Frame 030311/0942 →
CHANGE OF NAME Recorded Apr 29, 2013
From: MEDIMMUNE, INC.
To: MEDIMMUNE, LLC
Reel/Frame 030312/0012 →
Continuity (8)
Division 13192429 · Jul 27, 2011
Division 12691433 · Jan 21, 2010
Continuation 11649455 · Jan 3, 2007
Continuation 11397328 · Apr 3, 2006
Continuation 10020354 · Dec 12, 2001
Provisional Application 60254884 · Dec 12, 2000
Provisional Application 60289760 · May 9, 2001
Related Publication 20130052135A1 · Feb 28, 2013